Medical Device Manufacturer · BE , Gent-Zwijnaarde

Feops NV - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2021

4

Total

3

Cleared

1

Denied

FDA 510(k) Regulatory Record - Feops NV Radiology ✕

1 devices

1-1 of 1

Cleared Jun 06, 2023

FEops HEARTguideTM, FEops HEARTguideTM ALPACA

Radiology · 165d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026